Concentration-Dependent Control of the Band Gap Energy of a Low-Dimensional Lepidocrocite Titanate

Recently, we reported on the simple, scalable synthesis of quantum-confined one-dimensional (1D) lepidocrocite titanate nanofilaments (1DLs). Herein, we show, using solid-state UV–vis spectroscopy, that reducing the concentration of aqueous 1DL colloidal suspensions from 40 to 0.01 g/L increases the band gap energy and light absorption onset of dried filtered films from ≈3.5 to ≈4.5 eV. This range is ascribed to quantum confinement as the system transitions from two-dimensional (2D) into 1D with dilution. It is only after the colloidal suspensions are dried and the 1DLs start to self-assemble into ribbons and sheets that the band gap values change. This self-assembly is manifested in the X-ray diffraction patterns and the emergence of a Raman band characteristic of 2D lepidocrocite titanates. In colloidal form, 1DLs exhibit a lyotropic liquid crystal phase with a critical concentration of between 10 and 1 g/L. Additionally, the Beer–Lambert law applies with a mass absorbance coefficient of 2 ± 0.4 Lg^–1 cm^–1. The optical absorbance edges of the colloidal suspensions are not a function of concentration. The experimental findings are theoretically supported by density functional theory calculations of the Raman vibrational modes and electronic band structures of the 1D and 2D lepidocrocite titanate atomic structures.